All Stories

  1. Front Cover: Catechol‐Functionalized Carbon Nanotubes as Support for Pd Nanoparticles: a Recyclable System for the Heck Reaction (Eur. J. Org. Chem. 45/2022)
  2. Is a Catalyst Always Needed? The Case of the Knoevenagel Reaction with Malononitrile
  3. Is a Catalyst Always Needed? The Case of the Knoevenagel Reaction with Malononitrile
  4. Catechol‐Functionalized Carbon Nanotubes as Support for Pd Nanoparticles: a Recyclable System for the Heck Reaction
  5. New biocides based on imidazolinium-functionalised hybrid mesoporous silica nanoparticles
  6. Supported Poly(Ionic Liquid)-Heteropolyacid Based Materials for Heterogeneous Catalytic Fructose Dehydration in Aqueous Medium
  7. Low Angle Bending Detection Semi-transparent Piezoresistive Sensor
  8. First Evidence of Tris(catecholato)silicate Formation from Hydrolysis of an Alkyl Bis(catecholato)silicate
  9. Carbon nanotube supported aluminum porphyrin-imidazolium bromide crosslinked copolymer: A synergistic bifunctional catalyst for CO2 conversion
  10. White light emitting silsesquioxane based materials: the importance of a ligand with rigid and directional arms
  11. A Study on the Stability of Carbon Nanoforms–Polyimidazolium Network Hybrids in the Conversion of CO2 into Cyclic Carbonates: Increase in Catalytic Activity after Reuse
  12. Bending Sensors Based on Thin Films of Semitransparent Bithiophene‐Fulleropyrrolidine Bisadducts
  13. Reconsidering TOF calculation in the transformation of epoxides and CO2 into cyclic carbonates
  14. Tuneable Emission of Polyhedral Oligomeric Silsesquioxane Based Nanostructures that Self‐Assemble in the Presence of Europium(III) Ions: Reversible trans ‐to‐ cis Isomerization
  15. Straightforward preparation of highly loaded MWCNT–polyamine hybrids and their application in catalysis
  16. POSS nanostructures in catalysis
  17. Tuneable Emission of Polyhedral Oligomeric Silsesquioxane Based Nanostructures that Self‐Assemble in the Presence of Europium(III) Ions: Reversible trans ‐to‐ cis Isomerization
  18. Efficient Conversion of Carbon Dioxide by Imidazolium‐Based Cross‐Linked Nanostructures Containing Polyhedral Oligomeric Silsesquioxane (POSS) Building Blocks
  19. SBA‐15/POSS‐Imidazolium Hybrid as Catalytic Nanoreactor: the role of the Support in the Stabilization of Palladium Species for C−C Cross Coupling Reactions.
  20. Templating effect of carbon nanoforms on highly cross‐linked imidazolium network: Catalytic activity of the resulting hybrids with Pd nanoparticles
  21. Hybrid Catalysts for CO2 Conversion into Cyclic Carbonates
  22. Supported Polyhedral Oligomeric Silsesquioxane‐Based (POSS) Materials as Highly Active Organocatalysts for the Conversion of CO 2
  23. Modified Nanocarbons for Catalysis
  24. Cross-Linked Polyamine from Imidazolium-Based Materials: A Simple Route to Useful Catalytic Materials
  25. Enhanced power-conversion efficiency in organic solar cells incorporating copolymeric phase-separation modulators
  26. Supported Ionic Liquids: A Versatile and Useful Class of Materials
  27. Correction: Supported C60-IL-PdNPs as extremely active nanocatalysts for C–C cross-coupling reactions
  28. Imidazolium-Functionalized Carbon Nanohorns for the Conversion of Carbon Dioxide: Unprecedented Increase of Catalytic Activity after Recycling
  29. DNA-Binding and Anticancer Activity of Pyrene-Imidazolium Derivatives
  30. Sensor Properties of Pristine and Functionalized Carbon Nanohorns
  31. Advances in Organic and Organic-Inorganic Hybrid Polymeric Supports for Catalytic Applications
  32. Single-Walled Carbon Nanotube–Polyamidoamine Dendrimer Hybrids for Heterogeneous Catalysis
  33. Proximity Effect using a Nanocage Structure: Polyhedral Oligomeric Silsesquioxane-Imidazolium Tetrachloro- palladate Salt as a Precatalyst for the Suzuki-Miyaura Reaction in Water
  34. Highly Loaded Multi-Walled Carbon Nanotubes Non-Covalently Modified with a Bis-Imidazolium Salt and their Use as Catalyst Supports
  35. ChemInform Abstract: Covalently Supported Ionic Liquid Phases: An Advanced Class of Recyclable Catalytic Systems
  36. Covalently Supported Ionic Liquid Phases: An Advanced Class of Recyclable Catalytic Systems
  37. Supported C60-IL-PdNPs as extremely active nanocatalysts for C–C cross-coupling reactions
  38. ChemInform Abstract: A Simple Procedure for the Oxidation of Alcohols Using [Bis(acetoxy)iodo]benzene and a Catalytic Amount of Bromide Ions in Ethyl Acetate.
  39. Cross-Linked Thiazolidine Network as Support for Palladium: A New Catalyst for Suzuki and Heck Reactions
  40. A Simple Procedure for the Oxidation of Alcohols Using [Bis(acetoxy)iodo]benzene and a Catalytic Amount of Bromide Ions in Ethyl Acetate
  41. Thiazolium-Based Catalysts for the Etherification of Benzylic Alcohols under Solvent-Free Conditions
  42. Extremely water-soluble fullerenes
  43. Carbon Nanoforms can be easily functionalized with disulfides, diselenides and ditellurides
  44. A polyhedral oligomeric silsesquioxane-based catalyst for the efficient synthesis of cyclic carbonates
  45. Catalytic Synergism in a C60IL10TEMPO2Hybrid in the Efficient Oxidation of Alcohols
  46. Efficient microwave-mediated synthesis of fullerene acceptors for organic photovoltaics
  47. An E-Factor Minimized Protocol for a Sustainable and Efficient Heck Reaction in Flow
  48. Highly selective detection of Epinephrine at oxidized Single-Wall Carbon Nanohorns modified Screen Printed Electrodes (SPEs)
  49. Fullerene as a Platform for Recyclable TEMPO Organocatalysts for the Oxidation of Alcohols
  50. Evidences of release and catch mechanism in the Heck reaction catalyzed by palladium immobilized on highly cross-linked-supported imidazolium salts
  51. Recyclable Heterogeneous and Low‐Loading Homogeneous Chiral Imidazolidinone Catalysts for α‐Alkylation of Aldehydes
  52. ChemInform Abstract: Non‐Conventional Methods and Media for the Activation and Manipulation of Carbon Nanoforms
  53. ChemInform Abstract: Recyclable Catalyst Reservoir: Oxidation of Alcohols Mediated by Noncovalently Supported Bis(imidazolium)‐Tagged 2,2,6,6‐Tetramethylpiperidine 1‐Oxyl.
  54. Cross‐Linked Imidazolium Salts as Scavengers for Palladium
  55. Non-conventional methods and media for the activation and manipulation of carbon nanoforms
  56. ChemInform Abstract: Palladium Supported on Cross‐Linked Imidazolium Network on Silica as Highly Sustainable Catalysts for the Suzuki Reaction under Flow Conditions.
  57. ChemInform Abstract: “Release and Catch” Catalytic Systems
  58. Water in Organocatalytic Reactions
  59. Palladium Supported on Cross‐Linked Imidazolium Network on Silica as Highly Sustainable Catalysts for the Suzuki Reaction under Flow Conditions
  60. Recyclable Catalyst Reservoir: Oxidation of Alcohols Mediated by Noncovalently Supported Bis(imidazolium)‐Tagged 2,2,6,6‐Tetramethylpiperidine 1‐Oxyl
  61. An Atom‐Economical Approach to Functionalized Single‐Walled Carbon Nanotubes: Reaction with Disulfides
  62. An Atom‐Economical Approach to Functionalized Single‐Walled Carbon Nanotubes: Reaction with Disulfides
  63. ChemInform Abstract: “Nonsolvent” Applications of Ionic Liquids in Organocatalysis
  64. “Release and catch” catalytic systems
  65. Buckyballs
  66. ChemInform Abstract: A Liquid—Liquid Biphasic Homogeneous Organocatalytic Aldol Protocol Based on the Use of a Silica Gel Bound Multilayered Ionic Liquid Phase.
  67. ChemInform Abstract: Hydrogen Bonding Donor‐Acceptor Carbon Nanostructures
  68. ChemInform Abstract: Low‐Loading Asymmetric Organocatalysis
  69. A Straightforward Electroactive π‐Extended Tetrathiafulvalene (exTTF) Building Block
  70. A Liquid–Liquid Biphasic Homogeneous Organocatalytic Aldol Protocol Based on the Use of a Silica Gel Bound Multilayered Ionic Liquid Phase
  71. Carbon Nanostructures: Covalent and Macromolecular Chemistry
  72. ChemInform Abstract: Asymmetric Synthesis Using Polymer‐Immobilized Proline Derivatives
  73. “Nonsolvent” Applications of Ionic Liquids in Organocatalysis
  74. Low-loading asymmetric organocatalysis
  75. Multilayered Supported Ionic Liquids as Catalysts for Chemical Fixation of Carbon Dioxide: A High‐Throughput Study in Supercritical Conditions
  76. Polystyrene-supported organocatalysts for α-selenenylation and Michael reactions
  77. Multi‐Layered, Covalently Supported Ionic Liquid Phase (mlc‐SILP) as Highly Cross‐Linked Support for Recyclable Palladium Catalysts for the Suzuki Reaction in Aqueous Medium
  78. Catalytic Methods in Asymmetric Synthesis
  79. Recyclable Organocatalysts in Asymmetric Reactions
  80. Asymmetric Synthesis Using Polymer‐Immobilized Proline Derivatives
  81. ChemInform Abstract: Supported Organocatalysts as a Powerful Tool in Organic Synthesis
  82. Chapter 4. Fullerene-Containing Polymers
  83. Chapter 6. Hydrogen Bonding Donor–Acceptor Carbon Nanostructures
  84. New Concepts and Applications in the Macromolecular Chemistry of Fullerenes
  85. Advances towards Highly Active and Stereoselective Simple and Cheap Proline‐Based Organocatalysts
  86. Supported Organocatalysts as a Powerful Tool in Organic Synthesis
  87. ChemInform Abstract: Enhanced Activity and Stereoselectivity of Polystyrene‐Supported Proline‐Based Organic Catalysts for Direct Asymmetric Aldol Reaction in Water.
  88. Asymmetric Aldol Reaction with Polystyrene-Supported Proline-Based Catalysts
  89. Enhanced Activity and Stereoselectivity of Polystyrene‐Supported Proline‐Based Organic Catalysts for Direct Asymmetric Aldol Reaction in Water
  90. Fullerene Polymers
  91. Fullerene‐Containing Polymers: An Overview
  92. Main‐Chain and Side‐Chain C 60 ‐Polymers
  93. ChemInform Abstract: Water in Stereoselective Organocatalytic Reactions
  94. ChemInform Abstract: New Simple Hydrophobic Proline Derivatives as Highly Active and Stereoselective Catalysts for the Direct Asymmetric Aldol Reaction in Aqueous Medium.
  95. Water in Stereoselective Organocatalytic Reactions
  96. New Simple Hydrophobic Proline Derivatives as Highly Active and Stereoselective Catalysts for the Direct Asymmetric Aldol Reaction in Aqueous Medium
  97. ChemInform Abstract: Supported Proline and Proline‐Derivatives as Recyclable Organocatalysts
  98. ChemInform Abstract: Novel Prolinamide‐Supported Polystyrene as Highly Stereoselective and Recyclable Organocatalyst for the Aldol Reaction.
  99. Direct Asymmetric Aldol Reaction Using Polystyrene-Supported Proline Amide
  100. ChemInform Abstract: First Evidence of Proline Acting as a Bifunctional Catalyst in the Baylis—Hillman Reaction Between Alkyl Vinyl Ketones and Aryl Aldehydes.
  101. Novel Prolinamide‐Supported Polystyrene as Highly Stereoselective and Recyclable Organocatalyst for the Aldol Reaction
  102. ChemInform Abstract: New Ionic Liquid‐Modified Silica Gels as Recyclable Materials for L‐Proline‐ or H—Pro—Pro—Asp—NH2‐Catalyzed Aldol Reaction.
  103. Polystyrene-supported proline as recyclable catalyst in the Baylis–Hillman reaction of arylaldehydes and methyl or ethyl vinyl ketone
  104. First Evidence of Proline Acting as a Bifunctional Catalyst in the Baylis–Hillman Reaction Between Alkyl Vinyl Ketones and Aryl Aldehydes
  105. ChemInform Abstract: Hydrophobically Directed Aldol Reactions: Polystyrene‐Supported L‐Proline as a Recyclable Catalyst for Direct Asymmetric Aldol Reactions in the Presence of Water.
  106. Supported proline and proline-derivatives as recyclable organocatalysts
  107. Heterogeneous Catalytic Asymmetric Direct Aldol Reaction in Water
  108. Fullerene Polymers: Synthetic Strategies, Properties and Applications
  109. Hydrophobically Directed Aldol Reactions: Polystyrene‐Supported L‐Proline as a Recyclable Catalyst for Direct Asymmetric Aldol Reactions in the Presence of Water
  110. Hydrophobically Directed Aldol Reactions: Polystyrene‐Supported L‐Proline as a Recyclable Catalyst for Direct Asymmetric Aldol Reactions in the Presence of Water (Eur. J. Org. Chem. 28/2007)
  111. Fullerene Polymers: Synthesis and Properties
  112. Polystyrene‐Supported Proline and Prolinamide. Versatile Heterogeneous Organocatalysts Both for Asymmetric Aldol Reaction in Water and α‐Selenenylation of Aldehydes.
  113. Asymmetric Aldol Reaction in Water Catalyzed by Polystyrene-Supported Proline
  114. Chapter 6. Hydrogen Bonding Donor–Acceptor Carbon Nanostructures
  115. Polystyrene-supported proline and prolinamide. Versatile heterogeneous organocatalysts both for asymmetric aldol reaction in water and α-selenenylation of aldehydes
  116. Tetrathiafulvalene-based molecular nanowires
  117. New ionic liquid-modified silica gels as recyclable materials for l-proline- or H–Pro–Pro–Asp–NH2-catalyzed aldol reaction
  118. Cyclodextrin‐[6]fullerene Conjugates: Synthesis, Characterization, and Electrochemical Behavior.
  119. Fullerene Polymers:  Synthesis and Properties
  120. Cyclodextrin-[60]fullerene conjugates: synthesis, characterization, and electrochemical behavior
  121. Lipase-catalyzed resolution of anti-6-substituted 1,3-dioxepan-5-ols
  122. Long-Lived Photoinduced Charges in Donor−Acceptor Anthraquinone-Substituted Thiophene Copolymers
  123. Solid Film versus Solution‐Phase Charge‐Recombination Dynamics of exTTF–Bridge–C60 Dyads
  124. Topological Effects of a Rigid Chiral Spacer on the Electronic Interactions in Donor–Acceptor Ensembles
  125. Design, synthesis and photovoltaic properties of [60]fullerene based molecular materials
  126. Diphenylmethanofullerenes: New and Efficient Acceptors in Bulk-Heterojunction Solar Cells
  127. Cover Picture: Probing Molecular Wires: Synthesis, Structural, and Electronic Study of Donor–Acceptor Assemblies Exhibiting Long‐Range Electron Transfer (Chem. Eur. J. 16/2005)
  128. Probing Molecular Wires: Synthesis, Structural, and Electronic Study of Donor–Acceptor Assemblies Exhibiting Long‐Range Electron Transfer
  129. Concentration dependence of amplified spontaneous emission in two oligo-(p-phenylenevinylene) derivatives
  130. Electronic Communication through π‐Conjugated Wires in Covalently Linked Porphyrin/C60 Ensembles
  131. Mimicking photosynthesis: covalent [60]fullerene-based donor–acceptor ensembles
  132. Exceptionally Small Attenuation Factors in Molecular Wires
  133. Polymer solar cells with novel fullerene-based acceptor
  134. Donor?acceptor ?double-cable? polythiophenes with tunable acceptor content
  135. Tuning of the photoinduced charge transfer process in donor-acceptor double-cable copolymers
  136. Donor–acceptor polythiophene copolymers with tunable acceptor content for photoelectric conversion devices
  137. Tuning of the photoinduced charge transfer process in donor–acceptor double-cable copolymers
  138. Synthesis and Photoluminescent Properties of 1,1′‐Binaphthyl‐Based Chiral Phenylenevinylene Dendrimers.
  139. Synthesis of Soluble Donor−Acceptor Double-Cable Polymers Based on Polythiophene and Tetracyanoanthraquinodimethane (TCAQ)
  140. Synthesis and Photoluminescent Properties of 1,1‘-Binaphthyl-Based Chiral Phenylenevinylene Dendrimers
  141. ChemInform Abstract: Synthesis of 1,1′‐Binaphthyl‐Based Enantiopure C60 Dimers.
  142. Synthesis of 1,1‘-Binaphthyl-Based Enantiopure C60 Dimers